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Dual Analysis of Loss to Follow-up for Perinatally HIV-Infected Adolescents Receiving Combination Antiretroviral Therapy in Asia.
Bartlett, Adam W; Lumbiganon, Pagakrong; Jamal Mohamed, Thahira A; Lapphra, Keswadee; Muktiarti, Dina; Du, Quy Tuan; Hansudewechakul, Rawiwan; Ly, Penh Sun; Truong, Khanh Huu; Van Nguyen, Lam; Puthanakit, Thanyawee; Sudjaritruk, Tavitiya; Chokephaibulkit, Kulkanya; Do, Viet Chau; Kumarasamy, Nagalingeswaran; Nik Yusoff, Nik Khairulddin; Kurniati, Nia; Fong, Moy Siew; Wati, Dewi Kumara; Nallusamy, Revathy; Sohn, Annette H; Kariminia, Azar.
Afiliação
  • Bartlett AW; The Kirby Institute, UNSW Australia, Sydney, Australia.
  • Lumbiganon P; Department of Pediatrics, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
  • Jamal Mohamed TA; Pediatric Institute, Hospital Kuala Lumpur, Kuala Lumpur, Malaysia.
  • Lapphra K; Department of Pediatrics, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
  • Muktiarti D; Cipto Mangunkusumo-Faculty of Medicine Universitas Indonesia, Jakarta, Indonesia.
  • Du QT; Children's Hospital 1, Ho Chi Minh City, Vietnam.
  • Hansudewechakul R; Chiangrai Prachanukroh Hospital, Chiang Rai, Thailand.
  • Ly PS; National Centre for HIV/AIDS, Dermatology and STDs, Phnom Penh, Cambodia.
  • Truong KH; Children's Hospital 1, Ho Chi Minh City, Vietnam.
  • Van Nguyen L; National Hospital of Pediatrics, Hanoi, Vietnam.
  • Puthanakit T; The HIV Netherlands Australia Thailand Research Collaboration (HIV-NAT), The Thai Red Cross AIDS Research Centre, Bangkok, Thailand.
  • Sudjaritruk T; Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
  • Chokephaibulkit K; Department of Pediatrics, Faculty of Medicine, and Research Institute for Health Sciences, Chiang Mai University, Chiang Mai, Thailand.
  • Do VC; Department of Pediatrics, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
  • Kumarasamy N; Children's Hospital 2, Ho Chi Minh City, Vietnam.
  • Nik Yusoff NK; Chennai Antiviral Research and Treatment Clinical Research Site (CART CRS), VHS-Infectious Diseases Medical Centre, VHS, Chennai, India.
  • Kurniati N; Hospital Raja Perempuan Zainab II, Kelantan, Malaysia.
  • Fong MS; Cipto Mangunkusumo-Faculty of Medicine Universitas Indonesia, Jakarta, Indonesia.
  • Wati DK; Hospital Likas, Kota Kinabalu, Malaysia.
  • Nallusamy R; Sanglah Hospital, Udayana University, Bali, Indonesia.
  • Sohn AH; Penang Hospital, Penang, Malaysia.
  • Kariminia A; TREAT Asia/amfAR, The Foundation for AIDS Research, Bangkok, Thailand.
J Acquir Immune Defic Syndr ; 82(5): 431-438, 2019 12 15.
Article em En | MEDLINE | ID: mdl-31714422
ABSTRACT

BACKGROUND:

Perinatally HIV-infected adolescents (PHIVA) are an expanding population vulnerable to loss to follow-up (LTFU). Understanding the epidemiology and factors for LTFU is complicated by varying LTFU definitions.

SETTING:

Asian regional cohort incorporating 16 pediatric HIV services across 6 countries.

METHODS:

Data from PHIVA (aged 10-19 years) who received combination antiretroviral therapy 2007-2016 were used to analyze LTFU through (1) an International epidemiology Databases to Evaluate AIDS (IeDEA) method that determined LTFU as >90 days late for an estimated next scheduled appointment without returning to care and (2) the absence of patient-level data for >365 days before the last data transfer from clinic sites. Descriptive analyses and competing-risk survival and regression analyses were used to evaluate LTFU epidemiology and associated factors when analyzed using each method.

RESULTS:

Of 3509 included PHIVA, 275 (7.8%) met IeDEA and 149 (4.3%) met 365-day absence LTFU criteria. Cumulative incidence of LTFU was 19.9% and 11.8% using IeDEA and 365-day absence criteria, respectively. Risk factors for LTFU across both criteria included the following age at combination antiretroviral therapy initiation <5 years compared with age ≥5 years, rural clinic settings compared with urban clinic settings, and high viral loads compared with undetectable viral loads. Age 10-14 years compared with age 15-19 years was another risk factor identified using 365-day absence criteria but not IeDEA LTFU criteria.

CONCLUSIONS:

Between 12% and 20% of PHIVA were determined LTFU with treatment fatigue and rural treatment settings consistent risk factors. Better tracking of adolescents is required to provide a definitive understanding of LTFU and optimize evidence-based models of care.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções por HIV / Transmissão Vertical de Doenças Infecciosas / Antirretrovirais / Perda de Seguimento Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male / Pregnancy País como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções por HIV / Transmissão Vertical de Doenças Infecciosas / Antirretrovirais / Perda de Seguimento Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male / Pregnancy País como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article